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The VISERA ELITE™ III

Multispecialty Surgical Imaging Platform

The VISERA ELITE™ III platform delivers advanced imaging in true 4K centered around light, color, and clarity. It is the future-ready surgical imaging platform with software upgrades and technology that allows you to focus on your procedures, while reducing up-front and future costs.^*

Designed to meet the needs of multiple specialties like general surgery, urology, gynecology, ENT and more, the VISERA ELITE III platform offers 3D and 4K imaging, fluorescence-guided surgery (IR), Narrow Band Imaging™ (NBI™) Technology and Yellow Enhancement (YE) mode, all in one system. Benefit from compatibility with scopes, camera heads, and ENDOEYE™ videoscopes to adjust your investment for efficiency.^**

* Data on file with Olympus as of 04/2025.

** Refer to the IFU for compatible devices

The VISERA ELITE III Imaging Platform is a compact, multispecialty imaging platform designed for laparoscopic diagnosis, treatment, and video observation. TYPE BF endoscopes connected to this imaging platform must never be applied directly to the heart. Leakage current from the TYPE BF applied part may be dangerous and cause ventricular fibrillation or otherwise seriously affect the cardiac function of the patient.

EVIS X1™ Endoscopy System

Elevating the Standard of Care

The EVIS X1™ CV-1500 Video System Center combines a video processor and 5-LED light source in one box, resulting in a compact and lightweight design.¹ The CV-1500 features multiple special observation modes that support physicians during endoscopic procedures. In addition to conventional white light and Narrow Band Imaging™ (NBI™) technology, the CV-1500 offers three other enhanced observations to help improve diagnostic and therapeutic capability:

TXI™ technology (Texture & Color Enhancement Imaging) optimizes the structure, color tone and brightness of the mucosal surface.²
RDI™ technology (Red Dichromatic Imaging) designed to enhance the visibility of deep blood vessels and bleeding points.²
BAI-MAC™ (Brightness Adjustment Imaging with Maintenance of Contrast) technology designed to correct the brightness in darker portions of the image, while maintaining the brightness of the brighter portions of the image to increase visibility of distant areas.³
With One-touch Connector and no need for white balance adjustment,⁴ setup is simplified, with the aim of streamlining workflow and potentially accelerating procedure time. Touch panel allows the user to initiate all procedures and settings and control image data from one device,⁵ while convenient functions like Pre-freeze and MyCV mode assist in creating a user-friendly working environment. Downtime may be reduced by utilizing LED bulbs that are designed to last for years without needing replacement.⁶

The EVIS X1™ endoscopy system is not designed for cardiac applications. Other combinations of equipment may cause ventricular fibrillation or seriously affect the cardiac function of the patient. Improper use of endoscopes may result in patient injury, infection, bleeding, and/or perforation. Complete indications, contraindications, warnings, and cautions are available in the Instructions for Use (IFU). TXI, RDI, NBI and BAI-MAC technologies are not intended to replace histopathological sampling as a means of diagnosis.

Endoscopy and Infrared Fluorescence

Intraoperative endoscopy is an effective mitigation strategy for anastomotic leak prevention. When paired with infrared fluorescence technology, surgeons can assess anastomoses and staple lines endolumenally for mechanical failures, as well as laparoscopically for real-time perfusion assessments.

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ESG-410 Surgical Energy Platform

The ESG-410 Surgical Energy Platform powers the complete Olympus^® advanced energy portfolio, including hybrid and ultrasonic devices as well as your standard monopolar and bovie accessories.
It delivers monopolar, bipolar, advanced bipolar, ultrasonic, and hybrid energy to service multiple applications and is designed to support an efficient workflow across multiple surgical specialities.

The use of incompatible/non-validated equipment with the ESG-410 electrosurgical generator can lead to excessive/incorrect HF output. This can result in thermal injuries or death to the patient, and the operator as well as damage to the system.

POWERSEAL™ Portfolio

The POWERSEAL™ Sealer/Divider was built on a foundation of form and function you're used to, then enhanced to provide an improved ergonomic experience¹³ and accommodate your surgical preferences and technique.

Reliable 7 mm vessel sealing¹²
Improved ergonomics¹³
Three different jaw designs across the 5 mm portfolio
Secure tissue grasping and efficient dissection¹¹

Curved Jaw, Double-action

Curved Jaw, Single-action

Straight Jaw, Double-action

Open Extended Jaw

The POWERSEAL™ Sealer/Divider is a bipolar electrosurgical instrument indicated for use in a variety of procedures and specialties, and can be used on vessels up to and including 7 mm, lymphatics, and tissue bundles. The POWERSEAL device is intended for single use only, and has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures. Consult with a qualified professional prior to utilizing on patients who have electronic implants to avoid possible hazard.

THUNDERBEAT™ Portfolio

The THUNDERBEAT™ device is the only hybrid energy device on the market,⁷ offering the versatility and value of multiple devices in a single instrument.

Precise fine dissection⁸
Tip cutting ability⁸
Secure tissue grasping⁸
Easy entry into tight anatomy⁸
Blunt tissue dissection⁸
Minimal thermal spread⁸

THUNDERBEAT™
Open Extended Jaw Device

Designed for open procedures such as myomectomy and bowel resection

THUNDERBEAT™
Open Fine Jaw Type X Device

Designed for precise open procedures such as thyroidectomy

The THUNDERBEAT™ devices are hybrid ultrasonic and bipolar electrosurgical hand instruments intended for use in a variety of open and laparoscopic procedures to cut, seal, coagulate, and dissect with two distinct modes of action: Seal & Cut and Seal only. The devices can be used to seal vessels up to and including 7 mm, lymphatics, and tissue bundles. The THUNDERBEAT device is intended for single use only and has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures.

SONICBEAT™ Portfolio

The SONICBEAT portfolio is an ideal ultrasonic choice, combining precision and tissue control to help you achieve your clinical, operational, and financial goals.

Secure tissue grasping⁹
Precise fine dissection⁹
Minimal thermal spread⁹
5mm vessel sealing⁹
Reduced mist⁹

45 cm

35 cm

20 cm

The SONICBEAT device is intended to be used with the Ultrasonic Generator and the SONICBEAT Transducer for open, laparoscopic including single-site surgery, and general surgery to cut, dissect, coagulate, or grasp soft tissue or to seal and cut vessels in gynecologic, thoracic, urologic, and endoscopic surgical procedures. The SONICBEAT device has not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures, and should not be used for these procedures.

nCare™ 4K Medical Recorder

Medical recorder that captures high-resolution images and high-definition video from up to two surgical devices simultaneously.
Easily, reliably, and securely connect clinicians with the critical visual information they need with this user-friendly solution that can fit nearly anywhere from an endoscopic cart to an OR equipment boom.

Video recordings and images captured by the nCare 4K Medical Video Recorder are only intended for documentation of medical surgical procedures and are NOT to be used for diagnosis or treatment.

ES-IP™ System

The ES-IP system is a modular, scalable, work-flow based solution.

4K, fiber-based, enterprise-driven platform, the system is designed for ease of use and to help the surgical team focus on what matters most – the patient.
Vendor neutral and designed to integrate past, present, and future devices.
Seamless integration with VaultStream™ service to EHR vendors, MIMPS/PACS, and VNAs.
Intuitive touch screen interface designed for ease of use follows the natural workflow of surgery.
Windows IoT platform with Automated Software Update Service capability helps keep antivirus and ransomware protections up to date.
Third-party penetration tested to check for exploitable vulnerabilities in devices and web applications.¹⁰

Videos streamed/captured, and images captured by the ES-IP system and sent to the Electronic Health Record Systems by the VaultStream™ server software are only intended for documentation of medical surgical procedures and for the exchange of information are NOT to be used for diagnosis or treatment.

OR-VAC™ Surgical Smoke Plume Evacuator

The OR-VAC is intended to evacuate and filter surgical smoke and aerosols created by the interface of surgical tools with tissue (examples: lasers, electrosurgery systems, and ultrasonic devices).

The OR-VAC™ Surgical Smoke evacuator is intended to evacuate and filter surgical smoke and aerosols created by the interface of surgical tools with tissue. Make sure to inspect the surgical smoke evacuator before use to ensure there is no damage. Read and understand all warnings, contraindications, and instructions prior to use.

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Data on file with Olympus (DC00436067).
Data on file with Olympus (DC00489968).
Data on file with Olympus (DC00436067).
Olympus 1100 series endoscopes only, data on file with Olympus (DC00436067).
Data on file with Olympus (DC00460933).
Data on file with Olympus (DC00412083 and DC00623365).
As of September 2025.
Data on file with Olympus as of August 2017.
Data on file with Olympus as of January 2012.
Data on file with Olympus (DN0063585).
Data on file with Olympus (DN0049019, DN0044691, DN0044403).
Data on file with Olympus (DN0044249, DN0044289, DN0044705).
POWERSEAL CJSA data on file with Olympus (DN0046457).

Complete instructions, indications, contraindications and warnings for use can be found in the product labeling that accompanied your product. CAUTION: Federal Law (USA) restricts these devices to sale by or on the order of a physician. Refer to package insert provided with the product for complete Indications for Use, Contraindications, Warnings, Precautions, and Adverse Events prior to using this product.

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See. Treat. Connect.™with Olympus